US11090289B2ActiveUtilityA1
Compositions and methods for blocking sodium channels
Assignee: UNIV VIRGINIA PATENT FOUNDATIONPriority: Jan 24, 2017Filed: Jan 24, 2018Granted: Aug 17, 2021
Est. expiryJan 24, 2037(~10.5 yrs left)· nominal 20-yr term from priority
A61K 31/4164C07D 233/64A61K 31/4184A61P 25/08
75
PatentIndex Score
1
Cited by
39
References
5
Claims
Abstract
The disclosure provides methods for treating a subject suffering from a disease associated with sodium channel activity. The method comprises administering to the subject a therapeutically effective amount of a compound according to Formula II or Formula III described in the specification, or a pharmaceutically acceptable salt, prodrug, tautomer, stereoisomer, hydrate, or solvate thereof.
Claims
exact text as granted — not AI-modifiedWe claim:
1. A method for treating a subject suffering from epilepsy, the method comprising administering to the subject a therapeutically effective amount of a compound according to Formula II, or a pharmaceutically acceptable salt, prodrug, tautomer, stereoisomer, hydrate, or solvate thereof:
wherein
R1, R2, R3, R4, R5, R8 and R12 in each occurrence is independently H, CH 3 , F, Cl, Br, I, OCH 3 , CF 3 , OCF 3 , NH 2 , COOH, CHO, OH, SH, NO 2 , COCH 3 , CONH 2 , or NHCOCH 3 ;
R9, R10 and R11 each is independently H, CH 3 , F, Cl, Br, I, OCH 3 , CF 3 , OCF 3 , NH 2 , COOH, CHO, OH, SH, NO 2 , COCH 3 , CONH 2 , NHCOCH 3 , or
and
R13 is optionally substituted C 1 -C 6 alkyl, optionally substituted C 1 -C 6 haloalkyl, or halogen.
2. The method of claim 1 , wherein R13 is optionally substituted C 1 -C 6 alkyl.
3. The method of claim 2 , wherein R13 is CH 3 .
4. The method of claim 3 , wherein the compound has the structure:
or a pharmaceutically acceptable salt, prodrug, tautomer, stereoisomer, hydrate, or solvate thereof.
5. The method of claim 1 , wherein the epilepsy is partial epilepsy, generalized absence epilepsy, temporal lobe epilepsy or therapy resistant epilepsy.Join the waitlist — get patent alerts
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